The chemistry of bowtiene (tricyclo[5.3.0.02,6]decapentaene): a computational study

Abstract

Reactions of bowtiene (tricyclo[5.3.0.02,6]decapentaene, cyclobuta[1,2:3,4]dicyclopentene, bicyclopentadienylene, a tricyclic analogue of [10]annulene), in the sphere of unimolecular decomposition and dimerization were studied computationally to gauge its stability and reactivity, which are relevant to its feasability as a synthetic goal. The intuitively likeliest rearrangement mode to give species of lower energy begins with rearrangement to the 1,5-dehydronaphthalene diradical; this was calculated to have a barrier of approximately 220 kJ mol−1, too high for reaction at room temperature. Nevertheless, the energetics of rearrangement of the 1,5-diradical to the monocyclic 1,6-didehydro[10]annulene, a species of interest regarding its relationship to bowtiene and the diradical, were studied. The energy of bowtiene was compared with that of several other tricyclic 10π C10H6 cyclic polyenes.